- Serial CT Findings of Resolving Extramedullary Hematopoiesis as Unilateral Posterior Mediastinal Mass after Splenectomy in Hereditary Spherocytosis: A Case Report
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Nam MY, Lee JW, Kim YJ, Kim YJ, Kang YH, Lee KH
- KMID: 1439423
- J Korean Soc Radiol.
- 2012 Mar;66(3):263-266.
- doi: 10.3348/jksr.2012.66.3.263
Intrathoracic extramedullary hematopoiesis (EMH) is a rare condition of the hereditary spherocytosis. EMH usually regresses or disappears after treatment; such as splenectomy in the case of spherocytosis. We report a... -
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- Flow-Assisted Differential Diagnosis of Hemolytic Anemia with Spherocytosis: A Case Report
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Won DI
- KMID: 1781638
- Korean J Lab Med.
- 2010 Aug;30(4):339-344.
- doi: 10.3343/kjlm.2010.30.4.339
In patients with hemolytic anemia associated with spherocytosis, differential diagnosis has to be made whether the hemolysis is immune-mediated or of non-immune origin. We report a case of hereditary spherocytosis... -
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- Prolonged Extreme Thrombocytosis in a Postsplenectomy Patient with Hereditary Spherocytosis
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Park YM, Park J, Jo Y, Kim SH, Shin KC, Won IS, Sym SJ, Cho EK, Shin DB, Lee JH
- KMID: 2252116
- Korean J Hematol.
- 2009 Dec;44(4):298-303.
- doi: 10.5045/kjh.2009.44.4.298
We report a case of prolonged extreme reactive thrombocytosis in a post-splenectomy patient with hereditary spherocytosis. A 29-year-old female patient presented with gall stones detected incidentally by abdominal ultrasonography. Her... -
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- Extramedullary Hematopoiesis at the Posterior Mediastinum in Patient with Hereditary Spherocytosis: A Case Report
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Yeom SY, Lim JH, Han KN, Kang CH, Park IK, Kim YT
- KMID: 1427814
- Korean J Thorac Cardiovasc Surg.
- 2013 Apr;46(2):156-158.
- doi: 10.5090/kjtcs.2013.46.2.156
Thoracic extramedullary hematopoiesis (EMH) is a rare disease entity that is usually associated with hematologic disorders, such as myelodysplastic or hemolytic disease. Because thoracic EMH is usually encountered as a... -
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- Hereditary Spherocytosis
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Park ES
- KMID: 2049272
- Clin Pediatr Hematol Oncol.
- 2012 Oct;19(2):57-63.
Hereditary spherocytosis is a hemolytic anemia caused by erythrocyte membrane deficiencies that lead to membrane destabilization and vesiculation. Abnormal spherocytes are trapped and destroyed in the spleen. Mutations in several... -
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- A Case of Hereditary Spherocytosis with Hemolytic Anemia due to Mycoplasma pneumonia
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Na HY, Shin SH, Lee KM, Kim KN
- KMID: 2278928
- Korean J Pediatr Infect Dis.
- 2009 Dec;16(2):215-219.
Mycoplasma pneumoniae is a common cause of community-acquired pneumonia in children, with a peak incidence at 5-14 years. Extrapulmonary manifestations occur in 20-25% of patients with M. pneumoniae infection. Most... -
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- A Case of Hereditary Spherocytosis Coexisting with Gilbert's Syndrome
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Lee MJ, Chang YH, Kang SH, Mun SK, Kim H, Han CJ, Kim J, Kang HJ
- KMID: 1501640
- Korean J Gastroenterol.
- 2013 Mar;61(3):166-169.
- doi: 10.4166/kjg.2013.61.3.166
We recently encountered a case of hereditary spherocytosis coexisting with Gilbert's syndrome. Patient was initially diagnosed with Gilbert's syndrome and observed, but other findings suggestive of concurrent hemolysis, such as... -
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- Autoimmune Hemolytic Anemia after Aplastic Crisis due to Parvovirus B19 Infection in a Patient with Hereditary Spherocytosis
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Song SA, Lee MY, Kim SH, Lee JY, Oh SH, Shin JH, Kim HR, Jun KR, Lee JN
- KMID: 2312200
- Lab Med Online.
- 2012 Jul;2(3):166-169.
Hereditary spherocytosis (HS) is a genetic disorder characterized by the production and destruction of spherocytes due to a deficiency of red cell membrane cytoskeletal proteins, resulting in the clinical presentation... -
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- Hereditary Spherocytosis Coexisting with UDP-Glucuronosyltransferase Deficiency Highly Suggestive of Crigler-Najjar Syndrome Type II
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Iijima S, Ohzeki T, Maruo Y
- KMID: 1779679
- Yonsei Med J.
- 2011 Mar;52(2):369-372.
- doi: 10.3349/ymj.2011.52.2.369
Patients with co-existing hereditary spherocytosis (HS) and UDP-glucuronosyltransferase 1A1 (UGT1A1) deficiency as Gilbert's syndrome (GS) have been reported, and previous studies have demonstrated an increased risk for developing gallstones in... -
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- A case of concomitant Gilbert's syndrome and hereditary spherocytosis
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Lee HJ, Moon HS, Lee ES, Kim SH, Sung JK, Lee BS, Jeong HY, Lee HY, Eu YJ
- KMID: 1717328
- Korean J Hepatol.
- 2010 Sep;16(3):321-324.
- doi: 10.3350/kjhep.2010.16.3.321
We describe moderate hyperbilirubinemia in a 28-year-old man who suffered from gallstones and splenomegaly, with combined disorders of hereditary spherocytosis (HS) and Gilbert's syndrome (GS). Since it is difficult to... -
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- An Adult with Aplastic Crisis induced by Human Parvovirus B19 as an Initial Presentation of Hereditary Spherocytosis
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Oh SE, Kim JH, Choi CH, Park KH, Jung JY, Park YI, Park MJ
- KMID: 1776706
- Korean J Intern Med.
- 2005 Mar;20(1):96-99.
- doi: 10.3904/kjim.2005.20.1.96
The association between aplastic crisis and human parvovirus (HPV) B19 infection is well described in patients with sickle cell anemia. This association has also been described, although much less frequently,... -
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- Abnormalities of erythrocyte membrane proteins in Korean patients with hereditary spherocytosis
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Lee YK, Cho HI, Park SS, Lee YJ, Ra E, Chang YH, Hur M, Shin HY, Ahn HS
- KMID: 1128625
- J Korean Med Sci.
- 2000 Jun;15(3):284-288.
- doi: 10.3346/jkms.2000.15.3.284
Hereditary spherocytosis (HS) is a common inherited erythrocyte membrane disorder characterized by chronic hemolytic anemia. Clinical manifestations and biochemical abnormalities of HS are heterogeneous. In this study, we investigated erythrocyte... -
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- A Case of Congenital Microspherocytosis Requiring Early Splenectomy
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Mong FC, Cho KS, Kim KY
- KMID: 693092
- Yonsei Med J.
- 1987 Sep;28(3):234-242.
- doi: 10.3349/ymj.1987.28.3.234
Microspherocytosis is known as a hallmark of hereditary spherocytosis (HS) which is one of the most common hemolytic anemias with a prevalence of one per 5000, and is inherited... -
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- Hereditary Spherocytosis in Children: Experiences in a Single Center
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Park EA, Kim MK, Park JK, Lee SY
- KMID: 2168941
- Clin Pediatr Hematol Oncol.
- 2010 Oct;17(2):137-146.
PURPOSE: The aim of this study was to evaluate the clinical and laboratory findings of hereditary spherocytosis (HS) by comparing patients of different age groups and profiling the outcomes of... -
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- Splenic infarction in a patient with autoimmune hemolytic anemia and protein C deficiency
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Park MY, Kim JA, Yi SY, Chang SH, Um TH, Lee HR
- KMID: 2251989
- Korean J Hematol.
- 2011 Dec;46(4):274-278.
- doi: 10.5045/kjh.2011.46.4.274
Splenic infarction is most commonly caused by cardiovascular thromboembolism; however, splenic infarction can also occur in hematologic diseases, including sickle cell disease, hereditary spherocytosis, chronic myeloproliferative disease, leukemia, and lymphoma.... -
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- Hereditary hemolytic anemia in Korea from 2007 to 2011: A study by the Korean Hereditary Hemolytic Anemia Working Party of the Korean Society of Hematology
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Park ES, Jung HL, Kim HJ, Park SS, Bae SH, Shin HY, Song SH, Koh KN, Lyu CJ, Lim YT, Han DK, Hah JO
- KMID: 2270708
- Blood Res.
- 2013 Sep;48(3):211-216.
- doi: 10.5045/br.2013.48.3.211
BACKGROUND: The number of patients diagnosed with hereditary hemolytic anemia (HHA) has increased since the advent of novel diagnostic techniques that accurately identify this disorder. Here, we report data from... -
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- Clinical Experiences of Laparoscopic Surgery in Children
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Hong YI, Park JH, Kim IS, Rhee JA, Kim SY
- KMID: 2004073
- J Korean Surg Soc.
- 2008 Jul;75(1):47-55.
PURPOSE: The indications for pediatric laparoscopic surgery are increasing according to the improvement of laparoscopic procedures and instruments and the increased knowledge of its safety and benefits. We summarized the... -
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